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Publié il y a 2 mois

Senior Product Manager - Falcon Writer

@ Veeva

Toronto, Ontario

TélétravailTemps plein4+ ans d’expérience
Postuler
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En bref

Veeva is hiring a Senior Product Manager for Falcon Writer, its AI authoring product that drafts submittable regulated life sciences documents from customer data. The role owns core product features end to end, works with medical writing, regulatory and clinical teams, and requires 4+ years of product management experience. The posting offers a base salary of $130,000 to $180,000 CAD, a Work Anywhere arrangement, and a preference for candidates in Eastern or Central Time Zones.

Responsabilités :

  • Own and design Falcon Writer product features end to end
  • Turn early-stage problems into prioritized technical requirements
  • Work with medical writing, regulatory and clinical teams on document workflows
  • Define metrics for authoring speed, draft quality and adoption
  • Collaborate with Development, QA and Project Management

Résumé des exigences :

  • 4+ years of hands-on product management experience
  • Experience shipping AI or machine learning product features
  • Strong understanding of complex customer workflows
  • Extensive customer-facing experience and senior stakeholder alignment
  • A builder's instinct and comfort working hands-on with engineering

Outils et compétences

Avantages mentionnés

Assurance maladieSoins dentairesSoins de la vueAssurance vieRégime de retraiteCongés payés
Source et dates

Site carrière / système de candidatures · lever

Date publiée par l’employeur
2026-09-10
Première détection par notre source
2026-10-14
Mise à jour du dossier source
2026-10-29

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauSenior
DomaineOpérations
Expérience4 an(s) et plus
Heures par semaine40 (estimé)
Milieu de travailDomicile, Bureau
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
Avantages mentionnésCongés payés généreux, Régime de retraite

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Veeva

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

The Industry Cloud for Life Sciences

Description complète de l’entreprise

Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 1,500 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Canada, Europe, Asia, and Latin America. Visit the Jobs section for open positions and remember that correspondence to new applicants and existing candidates will only come from an official @veeva.com email address.

Abonnés LinkedIn
304 493
Personnes associées sur LinkedIn
9 835
Bureaux déclarés
  • 4280 Hacienda Drive, Pleasanton, CA 94588, US
  • Avinguda Diagonal 420, 2º 1ª C.P., Barcelona, 08037, ES
  • RM1823, 18F Bund Centre, 222 Yan An Rd. East, Huang Pu District Shanghai, 200002, CN
  • 〒160-0023 東京都新宿区西新宿, 6-10-1m 日土地西新宿ビル 8階, Tokyo, JP
  • 20 Toronto St, Toronto, ON M5C 2B8, CA
  • 131 Avenue Charles de Gaulle, Neuilly-sur-Seine, IdF 92200, FR
Autres noms enregistrés
  • Veeva Systems
Spécialités
  • Master Data Management
  • Regulatory
  • Quality
  • OpenData
  • Safety
  • R&D
  • Study Startup
  • Clinical Data Management
  • CTMS
  • Oncology Data
  • eTMF
  • Clinical Operations
  • Events Management
  • Territory Alignment
  • Multichannel CRM
  • Customer Reference Data
  • Cosmetics
  • Consumer Goods
  • Chemical
  • Animal Health
  • Remote Engage Meeting
  • Medical Devices
  • EDC
  • CDB
  • Vault Coder
  • Vault Payments
  • Vault QMS
  • Quality Docs
  • and Medcomms
Le profil indique une agence de recrutement
Non

Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 1,500 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Canada, Europe, Asia, and Latin America. Visit the Jobs section for…

ChampValeur
SecteurSoftware Development
Taille5,001-10,000 employees
Siège socialPleasanton, CA
Type d’organisationPublic Company
Fondée en2007
SpécialitésMaster Data ManagementRegulatoryQualityOpenDataSafetyR&DStudy StartupClinical Data ManagementCTMSOncology Data
Offres sur Jobsy28
LinkedInVoir la page
Description

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Falcon Writer is Veeva's AI authoring product for regulated life sciences content. It drafts submittable documents from a customer's own data, so medical writers can produce accurate, source-backed content far faster.

We are looking for a Product Manager to join the Falcon Writer team and own a core part of the product. You will work directly with medical writing, regulatory, and clinical teams at customer organizations to understand their workflows, then turn that into a roadmap engineering can build against. This is a hands-on role in applied AI, in a domain where correctness matters more than almost anything else. This role has a preference for candidates based in the Eastern or Central Time Zones.

What You’ll Do

  • Own and design product features from start to finish, including user stories, functional and non-functional requirements, feature specifications, and quality control checks. Turn ambiguous, early-stage problems into clear technical requirements and prioritized, shippable work.
  • Collaborate closely with Development, QA, Project Management, and Product Management to ensure products are built and delivered with quality.
  • Acquire deep subject matter expertise in medical writing and work directly with medical writers, regulatory, and clinical teams to understand their document workflows, source data, and compliance requirements in detail.
  • Define the metrics that matter, including authoring speed, draft quality, and adoption, and use them to drive prioritization.
  • Be accountable for the success of the product

Requirements

  • 4+ years of hands-on product management experience.
  • Experience shipping AI or machine learning product features, with the ability to define AI use cases that carry clear user and business value and to reason about how AI systems behave and where they need guardrails, verification, and human review.
  • Strong ability to understand complex customer workflows and ambiguous, early-stage problems, and translate them into clear product direction and solutions.
  • Extensive customer-facing experience, with clear, direct communication and the ability to independently lead customer discovery and align senior stakeholders and cross-functional teams.
  • A builder's instinct. You would rather be in the weeds with engineering than reviewing a roadmap deck.

Nice to Have

  • Experience in the Life Sciences industry, SaaS, and/or enterprise products.
  • Familiarity with regulatory, clinical, medical writing, or pharma document workflows such as clinical study reports, regulatory submissions, and periodic or annual reports.
  • Experience with content management or document generation products.
  • Experience with Veeva or Vault.
  • Familiarity with generative AI workflows such as prompt design, model evaluation, or AI-assisted authoring.
  • Experience building working prototypes with AI coding tools to test ideas quickly.

Interviewing with Veeva

    We value your time and believe in a transparent hiring process. Here is the process you can expect.

  • Follow the application process and submit your resume.
  • Within 3 days, you will receive a link to a personality assessment administered by a third party, unless you have already completed it with Veeva previously.
  • Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
  • If moving to the interview stage, the process is as follows:
    1. A conversation with the hiring manager
    2. A practical case exercise
    3. A final conversation with our group's Senior Leader.
  • Once all interviews are complete, the manager will be in touch with a final decision.

Perks & Benefits

  • Medical, dental, vision, and basic life insurance
  • PTO and company paid holidays
  • Retirement programs
  • 1% charitable giving program

Compensation

  • Base pay: $130,000 - $180,000 CAD
  • The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.

#LI-Remote

#LI-MidSenior

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at [email protected].

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